Soluble Recombinant Influenza Antigens

ABSTRACT

The present invention provides a recombinant soluble trimeric hemagglutinin (rHA) protein comprising a hemagglutinin ectodomain and an oligomerization domain. The rHA is produced as a soluble homotrimer, and may further comprises a signal peptide and/or an endoplasmic reticulum (ER) retention signal. The invention is also directed to nucleic acids encoding the rHA of the invention, as well as vectors and chimeric constructs comprising the nucleic acid. Methods of producing the rHA are also provided. The rHA described herein may be used to formulate influenza vaccines, or may be used to enrich existing vaccines.

FIELD OF THE INVENTION

The present invention relates to the production of soluble recombinant influenza antigens. More specifically, the present invention is directed to the production of soluble recombinant influenza antigens that retain immunogenicity.

BACKGROUND OF THE INVENTION

Influenza is the leading cause of death in humans due to a respiratory virus. Common symptoms include fever, sore throat, shortness of breath, and muscle soreness, among others. During flu season, influenza viruses infect 10-20% of the population worldwide, leading to 250-500,000 deaths annually.

Influenza viruses are classified into types A, B, or C, based on the nucleoproteins and matrix protein antigens present. Influenza type A viruses may be further divided into subtypes according to the combination of hemagglutinin (HA) and neuraminidase (NA) surface glycoproteins presented. HA governs the ability of the virus to bind to and penetrate the host cell. NA removes terminal sialic acid residues from glycan chains on host cell and viral surface proteins, which prevents viral aggregation and facilitates virus mobility. Currently, 16 HA (H1-H16) and 9 NA (N1-N9) subtypes are recognized. Each type A influenza virus presents one type of HA and one type of NA glycoprotein. Generally, each subtype exhibits species specificity; for example, all HA and NA subtypes are known to infect birds, while only subtypes H1, H2, H3, H5, N1 and N2 have been shown to infect humans. Influenza viruses comprising H5 and H7 are considered the most highly pathogenic forms of influenza A viruses, and are most likely to cause future pandemics.

Influenza pandemics are usually caused by highly transmittable and virulent influenza viruses, and can lead to elevated levels of illness and death globally. The emergence of new influenza A subtypes resulted in 4 major pandemics in the 20^(th) century. The Spanish flu, caused by an H1N1 virus, in 1918-1919 led to the deaths of over 50 million people worldwide between 1917 and 1920. The risk of the emergence of a new subtype, or of the transmission to humans of a subtype endemic in animals, is always present. Of particular concern is a highly virulent form of avian influenza (also called “bird flu”), outbreaks of which have been reported in several countries around the world. In many cases, this bird flu can result in mortality rates approaching 100% within 48 hours. The spread of the avian influenza virus (H5N1), first identified in Hong Kong in 1997, to other Asian countries and Europe has been postulated to be linked to the migratory patterns of wild birds.

There is increasing concern that the virus may become highly infectious for humans. The major problem for human health is the fact that influenza viruses are antigenically unstable, that is, they mutate rapidly. Should the avian influenza virus come into contact with human viruses, genetic reassortment of the avian virus could result in a highly pathogenic influenza virus that could causes severe disease or death in humans. Furthermore, such mutation could result in an influenza virus that is easily transmitted in humans.

The current method of combating influenza in humans is by annual vaccination. Each year, the World Health Organization selects 3 viral strains for inclusion in the annual influenza vaccine, which is produced in fertilized eggs. However, the number of vaccine doses produced each year is not sufficient to vaccinate the world's population. For example, Canada and the United-States obtain enough vaccines doses to immunize about one third of their population, while only 17% of the population of the European Union can be vaccinated. It is evident that current worldwide production of influenza vaccine would be insufficient in the face of a worldwide flu pandemic. Therefore, governments and private industry alike have turned their attention to the productions of effective influenza vaccines.

As previously mentioned, the current method of obtaining influenza virus vaccines is by production in fertilized eggs. The virus is cultured in fertilized eggs, followed by inactivation of the virus and purification of viral glycoproteins. While this method maintains the antigenic epitope and post-translational modifications, there are a number of drawbacks including the risk of contamination due to the use of whole virus and variable yields depending on virus strain. Sub-optimal levels of protection may result from genetic heterogeneity in the virus due to its introduction into eggs. Other disadvantages includes extensive planning for obtaining eggs, contamination risks due to chemicals used in purification, and long production times. Also, persons hypersensitive to egg proteins may not be eligible candidates for receiving the vaccine.

To avoid the use of eggs, influenza viruses have also been produced in mammalian cell culture, for example in MDCK or PERC.6 cells, or the like. Another approach is reverse genetics, in which viruses are produced by cell transformation with viral genes. These methods, however, also requires the use of whole virus as well as elaborate methods and specific culture environments.

The use of viral DNA as a vaccine has been explored. In this technology, protection is obtained by expression of viral antigens in human cells; the antigens are then recognized as foreign antigen, which leads to an specific antibody response. However, there exists the risk of oncogene activation from introduction of DNA into determinant portion of human cell genome—a significant drawback.

Vaccines comprising recombinant viral antigens expressed in viral DNA transformed insect or plant cells have also been prepared by Dow Agroscience (see, for example WO 2004/098530). While the risk associated with the use of live virus is avoided and the production process is shorter, protein conformation and post-translational modifications are affected. The scale-up and purification steps are also relatively complex as the antigens are associated with cellular membranes. In addition, the dose of baculovirus-recombinant HA required for effective immunization in animals is 10-fold higher than that of natural HA produced in fertilized eggs. In both cases, the levels of viral antigen expression are low.

In an effort to avoid the difficulties associated with purification of membrane proteins, Huang et al (2001, Vaccine, 19:2163-2171) replaced the transmembrane domain and the cytoplasmic tail of the measles HA with an ER retention signal. The resulting HA protein was produced in tobacco plant cells for the development of oral vaccine (edible vaccine). The HA expressed is not as strongly retained in the ER as it is with the transmembrane domain, thus simplifying the purification procedure. However, the natural trimeric form of HA cannot be formed in those conditions, which can affect the immunogenicity of the recombinant protein.

Saelens et al (1999, Eur. J. Biochm, 260:166-175) expressed an HA gene lacking the transmembrane domain in yeast (Pichia pastoris), leading to the secretion of monomeric HA. This form, however, was less immunogenic than the trimeric HA.

In order to protect the world population from influenza and to stave off future pandemics, vaccine manufacturers will need to develop effective, rapid methods producing vaccine doses. The current use of fertilized eggs to produce vaccines is insufficient and involves a lengthy process. Recombinant technologies offer promising approaches to the production of influenza antigens. However, the production of hemagglutinin has been limited to membrane-associated protein, which involves complex extraction processes with low yields, or to poorly-immunogenic soluble proteins.

SUMMARY OF THE INVENTION

The present invention relates to the production of soluble recombinant influenza antigens. More specifically, the present invention is directed to the production of soluble recombinant influenza antigens that retain trimeric assembly and immunogenicity.

It is an object of the present invention to provide soluble recombinant influenza antigens.

The present invention provides a recombinant hemagglutinin (rHA), comprising a hemagglutinin domain and an oligomerization domain. The rHA is produced as a soluble homotrimer. The protein may further comprise a signal peptide and/or an endoplasmic reticulum (ER) retention signal.

The present invention also provides a nucleotide sequence encoding the rHA as just described above.

The present invention further provides a nucleic acid sequence comprising a) a nucleotide sequence encoding a hemagglutinin domain; and b) a nucleotide sequence encoding an oligomerization domain. The nucleic acid encodes a soluble rHA that forms a homotrimer. The nucleic acid may further comprise a nucleotide sequence encoding a signal peptide and/or an endoplasmic reticulum (ER) retention signal.

The present invention also provides a vector comprising the nucleotide as described above.

The invention further provides a host cell expressing the rHA as described above, a host cell transformed with the nucleotide as just described above, or a host cell transformed with the vector as just described above.

It is also provided by the present invention, a method of producing a recombinant rHA protein. The method comprises providing a host cell with a vector comprising: a) a nucleotide sequence encoding a hemagglutinin domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer; and b) a nucleotide sequence encoding an oligomerization domain, then expressing the rHA.

The present invention further provides a method of expressing a recombinant hemagglutinin (rHA) within a plant. In a first step, a vector comprising a nucleotide sequence encoding a hemagglutinin domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer and a nucleotide sequence encoding an oligomerization domain, is introduced into a plant. In the step of introducing (step a), the nucleic acid may be introduced in the plant in a transient manner, or the nucleic acid is introduced in the plant so that it is stable.

The present invention also provides a method of producing a recombinant hemagglutinin (rHA) in a plant, comprising: a) introducing a nucleic acid sequence into the plant, or portion thereof, the nucleic acid sequence comprising a regulatory region operatively linked to a nucleotide sequence encoding a hemagglutinin domain and an oligomerization domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer; and b) growing the transgenic plant, thereby producing the rHA. In the step of introducing (step a), the nucleic acid may be introduced in the plant in a transient manner, or the nucleic acid is introduced in the plant so that it is stable.

rHA is a very complex molecule to produce. Expression levels and yields of recombinant HA from current production systems are low; and consequently the production costs are high. This is mostly due to the complex trimeric structure of the protein, which must undergo a complex process for assembly during its synthesis. Furthermore, HA is a large protein that has a transmembrane domain, and is highly glycosylated. Producing a soluble form of HA would allow production at higher levels and decrease the complexity of the purification process. This would have an important impact on production costs. Replacing the transmembrane domain with soluble α-helices or other secondary structure suitable to stabilize HA structurally compatible with the coiled-coil core of the ectodomain of the HA protein is shown to yield stable, soluble HA trimers. Such recombinant proteins can be used to enrich current influenza vaccines, or in the preparation of new vaccines.

This summary of the invention does not necessarily describe all features of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features of the invention will become more apparent from the following description in which reference is made to the appended drawings wherein:

FIG. 1 shows a schematic of the domains of the naturally occurring hemagglutinin (HA) protein.

FIG. 2 shows the amino acid sequence of the GCN4-pII peptide (SEQ ID NO:1).

FIG. 3 shows the amino acid and nucleotide sequences of PDI (SEQ ID NOs:6 and 7; (Genbank Accession Z11499), an alfalfa signal peptide. The PDI signal peptide is homologous to mouse ERp59. The BglII restriction site is indicated in bold.

FIG. 4 shows the amino acid sequence (SEQ ID NO:8) of HA from influenza strain A/New Caledonia/20/99 (H1N1) (Genbank Accession AY289929; Primary accession UniProt KB/TrEMBL: Q6WG00). The rHA signal peptide is shown in italics. The cleavage site of HA0 is indicated in bold and the fusion peptide is underlined. The transmembrane domain is shown in gray background.

FIG. 5 shows the amino acid sequences of various rHA constructs according to the present invention. The amino acid numbering has been adjusted according to the original amino acid numbering of HA. The PDI signal peptide is indicated in italics, the HA₀ cleavage site is shown in bold, the fusion peptide is underlined, and the stop codon is represented by *. FIG. 5A is the amino acid sequence (SEQ ID NO:9) of full length rHA comprising the PDI signal peptide and the transmembrane domain and cytoplasmic tail. The transmembrane domain is shown in gray background. FIG. 5B is the amino acid sequence (SEQ ID NO:10) of ER-retained rHA using the SEKDEL retention signal. The retention signal is shown in gray background. FIG. 5C is the amino acid sequence (SEQ ID NO:11) of ER-retained rHA using the HDEL retention signal. The retention signal is shown in gray background. FIG. 5D is the amino acid sequence (SEQ ID NO:12) of soluble rHA without the transmembrane domain. FIG. 5E is the amino acid sequence (SEQ ID NO:13) of soluble trimeric rHA using the GCN4-pII trimeric peptide. The GCN4-pII peptide is shown in gray background. FIG. 5F is the amino acid sequence (SEQ ID NO:14) of soluble trimeric rHA using the GCN4-pII trimeric peptide and retained in the ER. The GCN4-pII peptide is shown in gray background and the SKDEL retention signal is shown in italics. FIG. 5G is the amino acid sequence (SEQ ID NO:15) of soluble trimeric rHA using the PRD trimeric peptide. The PRD peptide is shown in gray background. FIG. 5H is the amino acid sequence (SEQ ID NO:16) of soluble trimeric rHA using the PRD trimeric peptide, and retained in the ER. The PRD peptide is shown in gray background and the retention signal is shown in italics.

FIG. 6 shows the nucleotide sequences of various fragments according to the present invention. The non-coding sequence is presented in small capitals and useful restriction sites are underlined. FIG. 6A shows the nucleotide sequence (SEQ ID NO:17) of the HA₀ gene fragment. FIG. 6B shows the nucleotide sequence (SEQ ID NO:18) of the transmembrane domain and the cytoplasmic tail gene fragment. FIG. 6C shows the nucleotide sequence (SEQ ID NO:19) of the ER-retained SEKDEL gene fragment. FIG. 6D shows the nucleotide sequence (SEQ ID NO:20) of the ER-retained HDEL gene fragment. FIG. 6E shows the nucleotide sequence (SEQ ID NO:21) of the GCN4-pII gene fragment. FIG. 6F shows the nucleotide sequence (SEQ ID NO:22) of the ER-retained GCN4-pII gene fragment. FIG. 6G shows the nucleotide sequence (SEQ ID NO:23) of the PRD gene fragment. FIG. 6H shows the nucleotide sequence (SEQ ID NO:24) of the ER-retained PRD gene fragment.

FIG. 7 is a schematic diagram of the rHA transfer DNA (t-DNA) in a pCAMBIA binary plasmid, in accordance with one embodiment of the present invention.

FIG. 8 is a Western blot showing the immunodetection of rHA expression in tobacco. Lanes: 1) Pure rHA standard (1 ng); 2) 1 ng of standard rHA spiked into 10 μg of plant extract; 3) 10 μg of plant extract; 4) 10 μg of protein extract from biomass expressing construct #540; 5) 10 μg of protein extract from biomass expressing construct #541; 6) 10 μg of protein extract from biomass expressing construct #542; 7) 10 μg of protein extract from biomass expressing construct #544; 8) 10 μg of protein extract from biomass expressing construct #545; 9) 10 μg of protein extract from biomass expressing construct #546; and 10) 10 μg of protein extract from biomass expressing construct #547.

FIG. 9 is a Western blot showing the immunodetection of rHA expression in tobacco, with 5 μg pf extract. FIG. 9A shows results from N. benthamiana, while FIG. 9B shows results from N. tabacum. Lanes: 1) 5 μg of plant extracts for panels B, D and A, C respectively; 2) 1 ng of standard rHA spiked into 2 and 5 μg of plant extract for panels B, D and A, C, respectively; 3) Extract from biomass expressing construct #540; 4) Extract from biomass expressing construct #541; 5) Extract from biomass expressing construct #542; 6) Extract from biomass expressing construct #544; 7) Extract from biomass expressing construct #545; 8) Extract from biomass expressing construct #546; and 9) Extract from biomass expressing construct #547.

FIG. 10 is a Western blot showing the immunodetection of rHA expression in tobacco, with 5 μg pf extract, under reducing conditions. FIG. 10A shows results from N. benthamiana, while FIG. 10B shows results from N. tabacum. Lanes: 1) 5 μg of plant extract; 2) 1 ng of standard rHA spiked into 5 μg of plant extract; 3) Extract from biomass expressing construct #540; 4) Extract from biomass expressing construct #541; 5) Extract from biomass expressing construct #542; 6) Extract from biomass expressing construct #544; 7) Extract from biomass expressing construct #545; 8) Extract from biomass expressing construct #546; and 9) Extract from biomass expressing construct #547.

FIG. 11 shows a plate with results of a hemagglutination assay. Row 1: PBS (Negative control); Row 2: PBS+1000 ng HA (PSC); Row 3: PBS+100 ng HA (PSC); Row 4: PBS+10 ng of HA (PSC); Row 5: PBS+1 ng of HA (PSC); Row 6: Non-transformed plant extract; Row 7: Non-transformed plant extract+1000 ng HA (PSC); Row 8: Non-transformed plant extract+100 ng HA (PSC); Row 9: Non-transformed plant extract+10 ng HA (PSC); Row 10: Non-transformed plant extract+1 ng HA (PSC); Row 11: Plant extract expressing construct 540 (transmembranar rHA); and Row 12: Plant extract expressing construct 544 (soluble rHA fused to GCN4).

DESCRIPTION OF PREFERRED EMBODIMENT

The present invention relates to the production of soluble recombinant influenza antigens. More specifically, the present invention is directed to the production of soluble recombinant influenza antigens that retain immunogenicity.

The following description is of a preferred embodiment.

The present invention provides a recombinant hemagglutinin (rHA) comprising a hemagglutinin domain and an oligomerization domain. The recombinant protein is produced as a soluble homotrimer. The rHA may also comprise a signal peptide and/or an endoplasmic reticulum (ER) retention signal.

Influenza is caused by influenza viruses, which are classified into types A, B, or C. Type A and B viruses are most often associated with epidemics. Influenza type A viruses may be further divided into subtypes according to the combination of hemagglutinin (HA) and neuraminidase (NA) surface glycoproteins presented. Currently, 16 HA (H1-H16) and 9 NA (N1-N9) subtypes are recognized. Each type A influenza virus presents one type of HA and one type of NA glycoprotein.

By the term recombinant hemagglutinin, also referred to as “recombinant HA” and “rHA”, it is meant a hemagglutinin protein that is produced by recombinant techniques, which are well known by a person of skill in the art. Hemagglutinin (HA) is an viral surface protein found on type A influenza viruses. To date, sixteen HA subtypes (H1-H16) have been identified. HA is responsible for binding of the virus to sialic acid residues of carbohydrate moieties on the surface of the infected host cell. Following endocytosis of the virus by the cell, the HA protein undergoes drastic conformational changes which initiate the fusion of viral and cellular membranes and virus entry into the cell.

HA is a homotrimeric membrane type I glycoprotein, generally comprising a signal peptide, a HA₀ domain, a membrane-spaning anchor site at the C-terminus and a small cytoplasmic tail (FIG. 1). The term “homotrimer” or “homotrimeric” indicates that an oligomer is formed by three HA protein molecules. HA protein is synthesized as a 75 kDa monomeric precursor protein (HA₀), which assembles at the surface into an elongated trimeric protein. Before trimerization occurs, the precursor protein HA0 is cleaved at a conserved activation cleavage site (also referred to as fusion peptide) into 2 polypeptide chains, HA1 (328 amino acids) and HA2 (221 amino acids), linked by a disulfide bond. Although this step is central for virus infectivity, it is not essential for the trimerization of the protein. Insertion of HA within the endoplasmic reticulum (ER) membrane of the host cell, signal peptide cleavage and protein glycosylation are co-translational events. Correct refolding of HA requires glycosylation of the protein and formation of 6 intra-chain disulfide bonds. The HA trimer assembles within the cis- and trans-Golgi complex, the transmembrane domain playing a role in the trimerization process. The crystal structures of bromelain-treated HA proteins, which lack the transmembrane domain, have shown a highly conserved structure amongst influenza strains (Russell et al. 2004). It has also been established that HA undergoes major conformational changes during the infection process, which requires the precursor HA₀ to be cleaved into the 2 polypeptide chains HA1 and HA2.

The recombinant HA of the present invention may be of any subtype. For example, the HA may be of subtype H1, H2, H3, H4, H5, H6, H7, H8, H9, H10, H11, H12, H13, H14, H15, or H16. The rHA of the present invention may comprise an amino acid sequence based on the sequence any hemagglutinin known in the art. Furthermore, the rHA may be based on the sequence of a hemagglutinin that is isolated from emerging influenza viruses.

The rHA of the present invention may be a chimeric protein construct comprising a hemagglutinin domain and an oligomerization domain. The term “hemagglutinin domain” refers to an amino acid sequence comprising either the HA₀ domain, or the HA1 and HA2 domains. In other words, the rHA protein may be processed (i.e., comprises HA1 and HA2 domains), or may be unprocessed (i.e., comprises the HA₀ domain). The hemagglutinin domain does not include the signal peptide, transmembrane domain, or the cytoplasmic tail found in the naturally occurring protein. The “oligomerization domain”, also referred to as “trimeric peptide”, refers to a domain that promotes the oligomerization of the rHA protein. The oligomerization domain may be any amino acid sequence known in the art that promotes the formation of trimers. For example, the oligomerization domain may be a heterologous peptide, for example, leucine zippers or peptides adopting a coiled-coil structure. The oligomerization domain may be of a length and/or structure similar to the transmembrane domain it replaces, which is 26 amino acids in length. Alternatively, the oligomerization domain may be of length and/or structure similar to the transmembrane domain (26 amino acids) and the cytoplasmic tail (10 amino acids) that it replaces. For example, and without wishing to be limiting, the oligomerization domain may be about 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47,4 8, 49, or 50 amino acids in length. In a specific, non-limiting example, the oligomerization domain is about 25-48 amino acids in length, or any amount therebetween. Non-limiting examples of suitable oligomerization domains include the GCN4-pII peptide (Harbury et al, 1993, Science, 262:1401-7), the proline-rich domain (PRD) of maize γ-zein, the bacteriophage T4 fibritin (Strelkov et al., 1996, Virology 219:190-194), or a trimerizing module identified in the fibronectin or collectin families.

In a specific, non-limiting example, the oligomerization domain may be the GCN4-pII peptide, a variant of the GCN4 yeast leucine zipper. This GCN4 mutant bears Ile residues at both a and d positions (pII), present at every 7 amino acids on the alpha-helix, leading to a high propencity for trimerization. The melting temperature (Tm) of the trimer is >100° C., conferring a high intrinsic stability to the oligomer (Harbour et al.). The amino acid sequence of GCN4-pII is shown in FIG. 2. GCN4-pII is well-suited for use as the oligomerization domain; the 29 amino acid sequence of GCN4-pII is placed at the C-terminal end of the HA domain sequence, essentially replacing the 26 amino acid transmembrane domain. If desired, additional amino acids may be placed at the C-terminal end of the rHA such that the recombinant structure does not terminate by an α-helix. For example, but without wishing to be limiting, Ser-Ala-Ala amino acid residues may be added at the C-terminal end of GCN4-pII.

In another example, the oligomerization domain may be the PRD of maize γ-zein, also referred to herein as “PRD”. Maize gamma-γ-Zein is known to store stacks in protein bodies once inside the ER. The synthetic PRD peptide adopts an amphipathic polyproline II conformation, which assembles itself as trimers (Kogan et al, 2002, Biophysical J., 83:1194-1204). In its natural form, the PRD comprises 8 repeats of the peptide PPPVHL (SEQ ID NO:2). The PRD peptide of maize gamma-γ-Zein is also placed at the C-terminus of the HA domain, replacing the transmembrane anchor. As the natural form of PRD is quite long, it is also within the scope of the present invention to provide the PRD in varying peptide lengths (4, 6 or 8 peptide repeats, i.e., 24, 36, or 48 amino acids in length). If desired, an amino acid linker may be placed between the HA domain and the PRD in order to permit the orientation of the PRD peptide chain towards a polyproline left helix. Any suitable peptide linker known in the art may be used. For example, and without wishing to be limiting in any manner, a tetrapeptide such as Gly-Gly-Ala-Gly (SEQ ID NO:3) may be used. Also if desired, additional amino acids may be placed at the C-terminal end of the rHA such that the recombinant structure does not terminate by an α-helix. For example, but without wishing to be limiting, Ser-Ala-Ala amino acid residues may be added at the C-terminal end of PRD.

In another non-limiting example, the oligomerisation domain may be the bacteriophage T4 fibritin (Strelkov et al., 1996, Virology 219:190-194). This domain comprises the last 29 amino acid residues at the C-terminal end of fibritin.

In yet another non limiting example, the oligomerization domain may be the trimerizing modules disclosed in WO 98/56906, incorporated herein by reference, which are trimerizing modules identified in the tetranectin family. The tetranectin trimerizing module also shows stability, in that its trimers were shown to exist at 60° C., or even 700° C. The trimerizing module may be covalently linked to the rHA, and is capable of forming a stable complex with two other trimerizing modules. Another example of oligomerization domain is the trimerizing peptides disclosed by WO 95/31540, incorporated herein by reference, which was identified in the collectin family. The peptides are about 25 to about 40 amino acids in length, and are derived from the neck region of proteins in the collectin family.

The rHA according to the present invention may further comprise a signal peptide. The signal peptide may be any suitable peptide known in the art, to direct the recombinant protein to the desired cell compartment or membrane. For example, and without wishing to be limiting, the signal peptide found in natural HA may be used, which directs HA the ER. In another non-limiting example, the signal peptide may be PDI, the alfalfa signal peptide. The amino acid and nucleotide sequences of PDI are shown in FIG. 3. Advantageously, the PDI signal peptide has a bg/II restriction site, which may be useful for cloning.

The rHA as described above may also further comprise an endoplasmic reticulum (ER) retention signal. Any suitable ER retention signal known by a person of skill in the art may be used. For example, but without wishing to be limiting in any manner, the Ser-Glu-Lys-Asp-Glu-Leu (SEKDEL; SEQ ID NO:4) or the His-Asp-Glu-Leu (HDEL; SEQ ID NO:5) ER retention signals may be used. The chosen ER retention signal may be at the C-terminal end of the rHA protein sequence. Advantageously, ER-retention of a recombinant protein in plants has been shown in several cases to improve the expression level by 2- to 10-fold (Schillberg et al, 2003, Cell Mol. Life Sci. 60:443-445). Without wishing to be bound by theory, the ER retention signals may allow back and forth movement of proteins between the ER and the Golgi complex, which allows trimerization to occur.

The term “soluble” indicates that the rHA is produced in the host cell in a soluble form. As described above, the conversion of recombinant HA to a soluble form arises from the replacement of the transmembrane hydrophobic domain by a soluble α-helices that are structurally compatible with the HA domain. Expressing the rHA in a soluble form may increase yields (higher expression levels) and decrease the complexity of purification, therefore lowering the production costs.

The present invention also provides a nucleic acid encoding the rHA as described above. The nucleic acid is a chimeric construct comprising a nucleotide sequence encoding a hemagglutinin domain (HA₀) and a nucleotide sequence encoding an oligomerization domain. The nucleic acid encoding the rHA may also comprise a nucleotide sequence encoding a signal peptide and/or a nucleotide sequence encoding an ER retention signal.

The present invention is further directed to a chimeric gene construct comprising a nucleic acid encoding rHA, as described above, operatively linked to a regulatory element. By “regulatory element” or “regulatory region”, it is meant a portion of nucleic acid typically, but not always, upstream of a gene, and may be comprised of either DNA or RNA, or both DNA and RNA. Regulatory elements may include those which are capable of mediating organ specificity, or controlling developmental or temporal gene activation. Furthermore, “regulatory element” includes promoter elements, core promoter elements, elements that are inducible in response to an external stimulus, elements that are activated constitutively, or elements that decrease or increase promoter activity such as negative regulatory elements or transcriptional enhancers, respectively. By a nucleotide sequence exhibiting regulatory element activity it is meant that the nucleotide sequence when operatively linked with a coding sequence of interest functions as a promoter, a core promoter, a constitutive regulatory element, a negative element or silencer (i.e. elements that decrease promoter activity), or a transcriptional or translational enhancer.

By “operatively linked” it is meant that the particular sequences, for example a regulatory element and a coding region of interest, interact either directly or indirectly to carry out an intended function, such as mediation or modulation of gene expression. The interaction of operatively linked sequences may, for example, be mediated by proteins that interact with the operatively linked sequences.

Regulatory elements as used herein, also includes elements that are active following transcription initiation or transcription, for example, regulatory elements that modulate gene expression such as translational and transcriptional enhancers, translational and transcriptional repressors, and mRNA stability or instability determinants. In the context of this disclosure, the term “regulatory element” also refers to a sequence of DNA, usually, but not always, upstream (5′) to the coding sequence of a structural gene, which includes sequences which control the expression of the coding region by providing the recognition for RNA polymerase and/or other factors required for transcription to start at a particular site. An example of a regulatory element that provides for the recognition for RNA polymerase or other transcriptional factors to ensure initiation at a particular site is a promoter element. A promoter element comprises a core promoter element, responsible for the initiation of transcription, as well as other regulatory elements (as listed above) that modify gene expression. It is to be understood that nucleotide sequences, located within introns, or 3′ of the coding region sequence may also contribute to the regulation of expression of a coding region of interest. A regulatory element may also include those elements located downstream (3′) to the site of transcription initiation, or within transcribed regions, or both. In the context of the present invention a post-transcriptional regulatory element may include elements that are active following transcription initiation, for example translational and transcriptional enhancers, translational and transcriptional repressors, and mRNA stability determinants.

The regulatory elements, or fragments thereof, may be operatively associated (operatively linked) with heterologous regulatory elements or promoters in order to modulate the activity of the heterologous regulatory element. Such modulation includes enhancing or repressing transcriptional activity of the heterologous regulatory element, modulating post-transcriptional events, or both enhancing/repressing transcriptional activity of the heterologous regulatory element and modulating post-transcriptional events. For example, one or more regulatory elements, or fragments thereof, may be operatively associated with constitutive, inducible, tissue specific promoters or fragment thereof, or fragments of regulatory elements, for example, but not limited to TATA or GC sequences may be operatively associated with the regulatory elements of the present invention, to modulate the activity of such promoters within plant, insect, fungi, bacterial, yeast, or animal cells

There are several types of regulatory elements, including those that are developmentally regulated, inducible and constitutive. A regulatory element that is developmentally regulated, or controls the differential expression of a gene under its control, is activated within certain organs or tissues of an organ at specific times during the development of that organ or tissue. However, some regulatory elements that are developmentally regulated may preferentially be active within certain organs or tissues at specific developmental stages, they may also be active in a developmentally regulated manner, or at a basal level in other organs or tissues within a plant as well.

By “promoter” it is meant the nucleotide sequences at the 5′ end of a coding region, or fragment thereof that contain all the signals essential for the initiation of transcription and for the regulation of the rate of transcription. There are generally two types of promoters, inducible and constitutive promoters. If tissue specific expression of the gene is desired, for example seed, or leaf specific expression, then promoters specific to these tissues may also be employed.

An inducible promoter is a promoter that is capable of directly or indirectly activating transcription of one or more DNA sequences or genes in response to an inducer. In the absence of an inducer the DNA sequences or genes will not be transcribed. Typically the protein factor that binds specifically to an inducible promoter to activate transcription is present in an inactive form which is then directly or indirectly converted to the active form by the inducer. The inducer can be a chemical agent such as a protein, metabolite, growth regulator, herbicide or phenolic compound or a physiological stress imposed directly by heat, cold, salt, or toxic elements or indirectly through the action of a pathogen or disease agent such as a virus. A plant cell containing an inducible promoter may be exposed to an inducer by externally applying the inducer to the cell or plant such as by spraying, watering, heating or similar methods. Examples of inducible promoters include, but are not limited to plant promoters such as: the alfalfa plastocyanine promoter (see, for example WO01/025455), which is light-regulated; the alfalfa nitrite reductase promoter (NiR; see for example W001/025454, which can be induced by fertilization with nitrates (3); and the alfalfa dehydrine promoter (U.S. Application Ser. No. 60/757,486), which is induced by environmental stresses such as cold.

A constitutive promoter directs the expression of a gene throughout the various parts of a plant and continuously throughout plant development. Any suitable constitutive promoter may be used to drive the expression of rHA within a transformed cell, or all organs or tissues, or both, of a host organism. Examples of known constitutive promoters include those associated with the CaMV 35S transcript. (Odell et al., 1985, Nature, 313: 810-812), the rice actin 1 (Zhang et al, 1991, Plant Cell, 3: 1155-1165) and triosephosphate isomerase 1 (Xu et al, 1994, Plant Physiol. 106: 459-467) genes, the maize ubiquitin 1 gene (Cornejo et al, 1993, Plant Mol. Biol. 29: 637-646), the Arabidopsis ubiquitin 1 and 6 genes (Holtorf et al, 1995, Plant Mol. Biol. 29: 637-646), and the tobacco translational initiation factor 4A gene (Mandel et al, 1995 Plant Mol. Biol. 29: 995-1004).

The term “constitutive” as used herein does not necessarily indicate that a gene is expressed at the same level in all cell types, but that the gene is expressed in a wide range of cell types, although some variation in abundance is often observed.

The chimeric gene construct of the present invention can further comprise a 3′ untranslated region. A 3′ untranslated region refers to that portion of a gene comprising a DNA segment that contains a polyadenylation signal and any other regulatory signals capable of effecting mRNA processing or gene expression. The polyadenylation signal is usually characterized by effecting the addition of polyadenylic acid tracks to the 3Y end of the mRNA precursor. Polyadenylation signals are commonly recognized by the presence of homology to the canonical form 5′ AATAAA-3′ although variations are not uncommon.

Examples of suitable 3′ regions are the 3′ transcribed non-translated regions containing a polyadenylation signal of Agrobacterium tumor inducing (Ti) plasmid genes, such as the nopaline synthase (Nos gene) and plant genes such as the soybean storage protein genes and the small subunit of the ribulose-1, 5-bisphosphate carboxylase (ssRUBISCO) gene. The 3′ untranslated region from the structural gene of the present construct can therefore be used to construct chimeric genes for expression in plants. Other examples of suitable 3′ regions are terminators, which may include, but are not limited to the noncoding 3′ region of the sequence of the plastocyanine or the nitrite reductase or the dehydrine alfalfa genes.

The chimeric gene construct of the present invention can also include further enhancers, either translation or transcription enhancers, as may be required. These enhancer regions are well known to persons skilled in the art, and can include the ATG initiation codon and adjacent sequences. The initiation codon must be in phase with the reading frame of the coding sequence to ensure translation of the entire sequence. The translation control signals and initiation codons can be from a variety of origins, both natural and synthetic. Translational initiation regions may be provided from the source of the transcriptional initiation region, or from the structural gene. The sequence can also be derived from the regulatory element selected to express the gene, and can be specifically modified so as to increase translation of the mRNA.

Also considered part of this invention are plants, portion or tissues of plants, plant cells, trees, portion of trees, tree cells, yeast, bacteria, fungi, insect and animal cells containing the chimeric gene construct comprising a nucleic acid encoding rHA, in accordance with the present invention. However, it is to be understood that the regulatory elements of the present invention may also be combined with coding region of interest for expression within a range of host organisms that are amenable to transformation. Such host organisms include, but are not limited to:

plants, both monocots and dicots, for example, corn, cereal plants, wheat, barley, oat, tobacco, Brassica, soybean, bean, pea, alfalfa, potato, tomato, ginseng, Arabidopsis; a portion or tissue of these plants for example, leaves, roots, stems, meristem, floral structure, cells of these plants and

yeast, fungi, insects, animal and bacteria cells.

Methods for the transformation and regeneration of these organisms are established in the art and known to one of skill in the art and the method of obtaining transformed and regenerated plants is not critical to this invention.

By “transformation” it is meant the interspecific transfer of genetic information (nucleotide sequence) that is manifested genotypically, phenotypically, or both. The interspecific transfer of genetic information from a chimeric construct to a host may be heritable and the transfer of genetic information considered stable, or the transfer may be transient and the transfer of genetic information is not inheritable.

Methods of regenerating whole plants from plant cells are also known in the art. In general, transformed plant cells are cultured in an appropriate medium, which may contain selective agents such as antibiotics, where selectable markers are used to facilitate identification of transformed plant cells. Once callus forms, shoot formation can be encouraged by employing the appropriate plant hormones in accordance with known methods and the shoots transferred to rooting medium for regeneration of plants. The plants may then be used to establish repetitive generations, either from seeds or using vegetative propagation techniques.

The constructs of the present invention can be introduced into plant cells using Ti plasmids, Ri plasmids, plant virus vectors, direct DNA transformation, micro-injection, electroporation, etc. For reviews of such techniques see for example Weissbach and Weissbach, Methods for Plant Molecular Biology, Academy Press, New York VIII, pp. 421-463 (1988); Geierson and Corey, Plant Molecular Biology, 2d Ed. (1988); and Miki and Iyer, Fundamentals of Gene Transfer in Plants. In Plant Metabolism, 2d Ed. D T. Dennis, D H Turpin, D D Lefebrve, D B Layzell (eds), Addison Wesly, Langmans Ltd. London, pp. 561-579 (1997). Other methods include direct DNA uptake, the use of liposomes, electroporation, for example using protoplasts, micro-injection, microprojectiles or whiskers, and vacuum infiltration. See, for example, Bilang, et al. (Gene 100: 247-250 (1991), Scheid et al. (Mol. Gen. Genet. 228: 104-112, 1991), Guerche et al. (Plant Science 52: 111-116, 1987), Neuhause et al. (Theor. Appl Genet. 75: 30-36, 1987), Klein et al., Nature 327: 70-73 (1987); Howell et al. (Science 208: 1265, 1980), Horsch et al. (Science 227: 1229-1231, 1985), DeBlock et al., Plant Physiology 91: 694-701, 1989), Methods for Plant Molecular Biology (Weissbach and Weissbach, eds., Academic Press Inc., 1988), Methods in Plant Molecular Biology (Schuler and Zielinski, eds., Academic Press Inc., 1989), Liu and Lomonossoff (J Virol Meth, 105:343-348, 2002,), U.S. Pat. Nos. 4,945,050; 5,036,006; and 5,100,792, U.S. patent application Ser. Nos. 08/438,666, filed May 10, 1995, and 07/951,715, filed Sep. 25, 1992, (all of which are hereby incorporated by reference).

As described below, transient expression methods may be used to express the constructs of the present invention (see Liu and Lomonossoff, 2002, Journal of Virological Methods, 105:343-348; which is incorporated herein by reference). Alternatively, a vacuum-based transient expression method, as described by Kapila et al., 1997, which is incorporated herein by reference) may be used. These methods may include, for example, but are not limited to, a method of Agro-inoculation or Agro-infiltration, syringe infiltration, however, other transient methods may also be used as noted above. With Agro-inoculation, Agro-infiltration, or synringe infiltration, a mixture of Agrobacteria comprising the desired nucleic acid enter the intercellular spaces of a tissue, for example the leaves, aerial portion of the plant (including stem, leaves and flower), other portion of the plant (stem, root, flower), or the whole plant. After crossing the epidermis the Agrobacteria infect and transfer t-DNA copies into the cells. The t-DNA is episomally transcribed and the mRNA translated, leading to the production of the protein of interest in infected cells, however, the passage oft-DNA inside the nucleus is transient.

To aid in identification of transformed plant cells, the constructs of the present invention may be further manipulated to include plant selectable markers. Useful selectable markers include enzymes which provide for resistance to an antibiotic such as gentamycin, hygromycin, kanamycin, and the like. Similarly, enzymes providing for production of a compound identifiable by colour change such as GUS (β-glucuronidase), or luminescence, such as luciferase are useful.

When specific sequences are referred to in the present invention, it is understood that these sequences include within their scope sequences that are “substantially homologous” to the specific sequences, or sequences or a compliment of the sequences hybridise to one or more than one nucleotide sequence as defined herein under stringent hybridisation conditions. Sequences are “substantially homologous” when at least about 70%, or more preferably 75% of the nucleotides match over a defined length of the nucleotide sequence providing that such homologous sequences exhibit one or more than one regulatory element activity as disclosed herein.

Such a sequence similarity may be determined using a nucleotide sequence comparison program, such as that provided within DNASIS (using, for example but not limited to, the following parameters: GAP penalty 5, # of top diagonals 5, fixed GAP penalty 10, k-tuple 2, floating gap 10, and window size 5). However, other methods of alignment of sequences for comparison are well-known in the art for example the algorithms of Smith & Waterman (1981, Adv. Appl. Math. 2:482), Needleman & Wunsch (J. Mol. Biol. 48:443, 1970), Pearson & Lipman (1988, Proc. Nat'l. Acad. Sci. USA 85:2444), and by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and BLAST, available through the NIH.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology, Ausubel et al., eds. 1995 supplement), or using Southern or Northern hybridization under stringent conditions (see Maniatis et al., in Molecular Cloning (A Laboratory Manual), Cold Spring Harbor Laboratory, 1982). Preferably, sequences that are substantially homologous exhibit at least about 80% and most preferably at least about 90% sequence similarity over a defined length of the molecule.

An example of one such stringent hybridization conditions may be overnight (from about 16-20 hours) hybridization in 4×SSC at 65° C., followed by washing in 0.1×SSC at 65° C. for an hour, or 2 washes in 0.1×SSC at 65° C. each for 20 or 30 minutes. Alternatively an exemplary stringent hybridization condition could be overnight (16-20 hours) in 50% formamide, 4×SSC at 42° C., followed by washing in 0.1×SSC at 65° C. for an hour, or 2 washes in 0.1×SSC at 65° C. each for 20 or 30 minutes, or overnight (16-20 hours), or hybridization in Church aqueous phosphate buffer (7% SDS; 0.5M NaPO₄ buffer pH 7.2; 10 mM EDTA) at 65° C., with 2 washes either at 50° C. in 0.1×SSC, 0.1% SDS for 20 or 30 minutes each, or 2 washes at 65° C. in 2×SSC, 0.1% SDS for 20 or 30 minutes each for unique sequence regions.

The rHA of the present invention can be used in conjunction with existing influenza vaccines, to supplement the vaccines, render them more efficacious, and to reduce the administration dosages necessary. As would be known to a person of skill in the art, the vaccine may be directed against one or more than one influenza virus. Examples of suitable vaccines include, but are not limited to those commercially available from Sanofi-Pasteur, ID Biomedical, Merial, Sinovac, Chiron, Roche, MedImmune, GlaxoSmithKline, and the like.

The invention will now be described in detail by way of reference only to the following non-limiting examples.

EXAMPLE 1 rHA Strategy

The HA chosen to exemplify the present invention was obtained from influenza strain A/New Caledonia/20/99 (H1N1). The A/New Caledonia/20/99 HA has been well characterized and immunodetection tools are commercially available. As the three-dimensional structures of all HAs are well conserved, the present expression strategy can directly apply to any other HA.

The expression of rHA was directed to the ER and the secretory pathway using the signal peptide of the alfalfa PDI (SEQ ID NO:3). This signal peptide was fused directly to the N-terminal primary sequence of mature rHA (FIG. 4; SEQ ID NO:8). The theoretical cleavage of the signal peptide from mature rHA with the PDI signal peptide was verified using the SignalP server 3.0.

rHA can be retained in the ER using the SEKDEL (SEQ ID NO:4) or the HDEL (SEQ ID NO:5) retention signals, both fused to the C-terminal end of rHA protein sequence.

When the GCN4-pII peptide was used as the oligomerization domain, it was fused directly to C-terminal of the last Tyr residue of HA₀. The Met residue at position 1 of GCN4-pII was changed to a Leu because Leu is more inert than Met and it has similar packing volume compared to the original Met. Amino acids Ser-Ala-Ala were added at the C-terminus of GCN4-pII.

When the PRD of maize gamma-γ-Zein was used, a peptide with 8 repetitions of the PPPVHL (SEQ ID NO:2) was fused to HA, to replace the transmembrane domain of HA. The 4 first proline residues were also included in the fusion. The C-terminal cysteine was excluded. To accommodate the fusion of a polyproline helix to the C-terminus of HA, the peptide Gly-Gly-Ala-Gly (SEQ ID NO:3) was added the N-terminal of PRD. The Ser-Ala-Ala peptide was added to the C-terminus of PRD.

In total, 8 different rHA gene constructs were prepared to test their expression in planta:

1. The full length rHA, including the transmembrane domain, with the PDI signal peptide (SEQ ID NO:9);

2. The transmembrane domain and cytoplasmic tail were removed from the rHA of item 1 and replaced by the retention signal SEKDEL (SEQ ID NO:10);

3. The transmembrane domain and cytoplasmic tail were removed from the rHA of item 1 and replaced by the retention signal HDEL (SEQ ID NO:11);

4. The transmembrane domain and cytoplasmic tail were removed from the rHA of item 1 (SEQ ID NO:12);

5. The transmembrane domain and cytoplasmic tails were removed from the rHA of item 1 and replaced by the GCN4-pII (SEQ ID NO:13);

6. The transmembrane domain and cytoplasmic tails were removed from the rHA of item 1 and replaced by the GCN4-pII, with the SEKDEL retention signal at the C-terminus (SEQ ID NO:14);

7. The transmembrane domain and cytoplasmic tails were removed from the rHA of item 1 and replaced by the PRD domain (SEQ ID NO:15); and

8. The transmembrane domain and cytoplasmic tails were removed from the rHA of item 1 and replaced by the PRD domain, with the SEKDEL retention signal at the C-terminus (SEQ ID NO:16).

EXAMPLE 2 Gene Synthesis

The eight different gene constructs described in Example 1 were synthesized. The wild-type nucleotide sequence of HA from influenza strain A/New Caledonia/20/99 was only modified to insert or remove restriction sites to facilitate the cloning steps. These minor modifications in the gene sequence did not change the resulting amino acid sequence of the protein. The HA₀ gene was synthesized with an ApaI restriction site at the 5′-end, in phase with the ATG of the PDI signal peptide. The 7 other genes bear a KpnI restriction site at their 5′-end. Every gene ends at the 3′ end with a stop codon (TAA), followed by a SacI and a StuI restriction sites. According to the designed cloning strategy, the following restriction sites were design to be unique in the final plasmid: ApaI, BstZ17 I, Sac I, Kpn I, Bgl II, and Stu I. The different gene fragments were synthesized at the Plant Biotechnology Institute and were delivered cloned into pUC18. Selected nucleotide sequence information is given in FIG. 6 (SEQ ID NOs:17-24).

EXAMPLE 3 Genetic Assembly of Vectors Expressing rHA Fusions

The various DNA constructs were assembled using known recombinant DNA techniques (Sambrook et al (1989) Molecular cloning: A laboratory Manual, Sec Ed. Cold Spring Harbor Laboratory press, Cold Spring Harbor, N.Y.). The E. coli DH5α strain was used has a host for amplification of the binary vectors, unless otherwise specified. The HA₀ gene fragment was ligated directly into the plastocynine cassette (already containing the pdi signal peptide) using the bglII and SacI restriction sites, or was co-ligated with the 7 other C-terminus ends using the KpnI, bglII and Sad restriction sites. In each case, the gene was inserted into a plastocyanine expression cassette contained on transfer DNA (t-DNA) of a binary vectors. t-DNA is the part of the binary vector that is integrated in the genome (from the right to the left border) of the host plant cell upon transformation. The binary vectors used in this example were derived from the commercial plasmid pCAMBIA 2300 (Cambia, Canberra, Au) and contained, from the right to left borders sequences of the t-DNA, the following elements:

various proprietary expression cassettes (promoter and terminator), available from Medicago, where the rHA genes are inserted;

a multiple cloning site to facilitate the cloning; and

the gene coding for neomycin phosphotansferase II (nptII), a selectable marker that confers resistance to kanamycin, under the control of a nopaline synthase (NOS) promoter and a cauliflower 35S mosaic virus (35S) terminator.

Each clone was submitted to DNA sequencing to verify the nucleotide sequence of the clones. Nucleotide variations were tolerated in the sequence of the rHA gene, provided the resulting amino acid sequence still encoded the exact same protein sequence (SEQ ID NOs:9-16). The 8 different DNA constructs are listed in Table 1, and an example of the resulting rHA t-DNA is shown schematically in FIG. 7.

TABLE 1 DNA constructs for rHA Sub-cellular ER retention SEQ ID No. Expression strategy targeting signal NO: 540 Complete transmembrane Apoplast 9 secreted 541 ER-retained ER SEKDEL 10 542 ER-retained ER HDEL 11 543 Soluble, secreted Apoplast 12 544 Soluble trimeric GCN4 Apoplast 13 545 Soluble trimeric GCN4 ER SEKDEL 14 546 Soluble trimeric PRD Apoplast 15 547 Soluble trimeric PRD ER SEKDEL 16

DNA isolated from E. coli proper clones was finally inserted into Agrobacterium tumefaciens Agl1 or other strains. The list of the Agrobacterium clones containing the various t-DNAs used in the present invention appears at Table 1. In preparation for plant transient expression experiments, plasmidic DNA was isolated from Agrobacterium clones and submitted restriction digest mapping to ensure integrity of the DNA

EXAMPLE 3 Transient Expression of rHA in Tobacco

Agrobacterium growth. The Agrobacterium clones containing a binary vector bearing rHA DNA constructs (Table 1) were grown for 24 hours at 28° C. in 2 mL of YEB or LB medium containing 25 and 50 μg/mL of each carbenicilin and kanamycin, respectively. 10 μL of these cultures were used as starting inoculums to generate cultures of 25 mL of YEB induction medium (YEB medium, 10 mM 2 (N morpholino) ethanesulfonic acid (MES), pH adjusted to 5.6, 25 mg/L carbenicillin, 50 mg/L kanamycin, 20 μM acetosyringone). The latter were grown in rotary shaker (220 rpm) incubator at 28° C. for 18 hours or until an optical density at 600 nm (OD600) of 0.8 to 1 was reached.

Growth of non-transgenic tobacco. Nicotiana benthamiana and Nicotiana tabacum plants were grown from seeds in a peat-based substrate (AgroMix) in a greenhouse. Seedlings were initially raised in a nursery and later transplanted to pots. Plants were irrigated twice a day and receive 180 ppm of nitrogen at each application. Greenhouse condition were kept at 25° C. during the day and 21° C. during the night, under a long day photoperiod regime (16 h light/8 h dark cycles), with artificial lightning of 20 watt m-2 at plant level.

Transient expression of rHA tobacco. The Agrobacterium culture prepared as described earlier was centrifuged 8 min at 10 000 g, resuspended in the same volume of inoculation medium (10 mM MgCl2, 10 mM MES, adjusted to pH 5.6, and supplemented with 100 μM acetosyringone) and kept at room temperature (RT, 23° C.) for 1 h prior to inoculation. Alternatively, the suspension can be kept at 4° C. for 24 hours prior to inoculation. Transient transformation of N. benthamiana and N. tabacum were essentially performed as described in Liu and Lomonossoff (2002, Journal of Virological Methods, 105:343-348), with the following modifications. For the expression of rHA, a mixture of two Agrobacteria strains was inoculated. The first strain contained one of the clones described at Table 1 and the second strain contained the HcPro suppressor of silencing from the Potato Virus Y under the control of the 35S promoter. After inoculation, the plants were incubated in a greenhouse. Temperature was kept at a minimum 23° C. during the day and 21° C. during the night. Plants were irrigated twice a day and received 180 ppm of nitrogen at each application. Harvest of biomass was undertaken after 4-8 days.

EXAMPLE 5 Demonstration of Expression of rHA in Tobacco Leaves

Preparation of a soluble protein extracts from inoculated leaves. Leaves were analyzed directly after harvesting or after freezing the biomass at −80° C. A vegetable biomass of Agro-inoculated leaves of ˜0.1 g was weighted and used for analysis of rHA transient expression.

One of two extraction methods was used to generate a total protein extract: by grounding the vegetable tissue with a mortar and a pestle, or by pulverizing it in a MixerMill300 (MM300) from Retsch. 0.1 g of plant biomass was transferred into a clean and pre-cooled mortar. 0.3 mL of cold extraction buffer (Tris 50 mM pH 7.4 containing NaCl 150 mM, 0.1% Triton X-100, and 5% glycerol) was added as well as PMSF and chymostatin to final concentrations of 1 mM and 10 μM, respectively. Leaves were ground with a pestle until a homogeneous preparation was obtained. The plant extract was then transferred into a 1.5 mL microtube and centrifuged at 20,000 g for 20 min at 4° C. Alternatively, 0.1 g of plant tissue with 0.3 mL of extraction buffer was introduced into non-sterile 1.5 microtube. A tungsten bead was added to each tube. The box was submitted to 3 min cycle of agitation at 30 Hz. The cycle was repeated 2 times. The plant extracts were then centrifuged as described above.

Following centrifugation, the supernatant was transferred into a clean microtube and maintained on ice. Finally, the total protein content of individual protein extracts was measured by the Bradford method using BSA as the reference protein.

Immunodetection of rHA transiently expressed in tobacco leaf material. The Agro-inoculated tobacco leaf protein extracts was prepared as described above. The following 3 controls were also prepared: 1) 1 ng of pure rHA (recombinant rHA produced by CHO cells, Protein Sciences Corporation, catalog # 3006) to which 1 μg of BSA (Pierce) was added, 2) 2-10 μg of tobacco protein extract obtained from a biomass agro-inoculated with agrobacteria transformed with an empty pCAMBIA plasmid, and 3) 1 ng of pure rHA spiked to 2-10 μg of the protein extract of sample #2.

Typically, 2-10 μg of protein extract from each biomass (transformed with one of the 8 different DNA constructs, see Table 1) was loaded on SDS-PAGE for Western blot analysis. Samples were boiled for 5 min at 100° C. prior to loading on denaturing SDS-PAGE (concentration 6% acrylamide; separation 10% acrylamide, Tris-glycine buffer) as essentially described by Thomas (1975, Proc. Nat. Acad. Sci. USA, 72:2626-2630). Electrophoresis was performed at 110 volts for 90 min using Mini Protean III apparatus (BioRad). Separated proteins were then blotted onto a PVDF membrane in a Tris 25 mM, Glyine 192 mM, Methanol 10% (v/v) pH 8.3 buffer at 100 V for 30 min or 60 min when using a Criterion blotter or a Mini-trans blot Unit (BioRad), respectively.

Immunodetection of rHA was achieved with the following antibodies. A mouse monoclonal antibody to influenza A virus (Fitzgerald Industries International Inc. Catalog # 10-I50) was used as the primary antibody at 1/1,000. The secondary antibody was a peroxidase conjugated goat anti-mouse IgG (H+L) (Jackson ImmunoResearch #111-035-146) used at 1/10,000. The peroxydase activity was detected using Immobilon Western Chemiluminescent HRP substrate (Milipore, catalog # WBRL50100) or BM chemiluminescent blotting substrate (POD) (Roche, catalog #11500 694 001).

The immunodetection method was optimized to obtain a specific signal against each rHA, without cross-reactivity with endogenous plant proteins. The limit of detection was low; which allowed detection of the proteins expressed at levels as low as >0.004% (1 ng into 25 μg of extract) of total soluble proteins (TSP).

As shown in FIG. 8, rHA was expressed in every condition tested and in both tobacco species. The use of non-reducing conditions allowed detection of different oligomeric forms of hemagglutinin: monomers, dimers and trimers. With decreasing quantities of protein loaded on the gel, as examplified at FIG. 9, the oligormeric forms of rHA are resolved. The latter are the same for every construct tested and in both tobacco species: immunodetection signals are observed at the level of the trimer and of the monomer. A third immunoreactive band is also observed, which migrates between the expected molecular weight of the dimer and that of the trimer.

The replacement of the transmembrane domain by the different trimeric coil-coiled peptides allowed expression of rHA with expression levels equal to or higher than the transmembrane form of rHA. This is especially true for the fusion with GCN4-pII. The fusion of rHA with the PRD allows expression at lower levels compared to the GCN4-pII fusion. The expression levels of the GCN4-pII-rHA fusion is of, at least, 0.01% TSP (>1 ng of rHA in 10 μg of TSP). Accumulation of rHA fusions appears higher in N. benthamiana compared to N. tabacum. Finally, retention of rHA to the ER, for every construct tested, increases significantly the expression levels of rHA. This tendency has been observed for many other proteins. The ER subcellular space is generally recognized for its low proteolytic activity compared to other compartments such as the apoplast, resulting in higher accumulation of recombinant proteins.

The same protein extracts were analysed under reducing conditions and immunodetected as described earlier to investigate whether the HA₀ chain is proteolysed into the two-chain form of rHA, i.e., HA1 and HA2. The expected molecular weights of the latter are 47 and 28 kDa, respectively. It is shown at FIG. 10 that the HA₀ is not readily converted to a two-chain form. It is worth noticing that proteolysis or clipping of rHA appears to be greater in the N. tabacum extracts.

EXAMPLE 6 Demonstration of Trimeric Assembly of rHA

Hemagglutination test. The hemagglutination assay was performed essentially as described by Nayak et al. (2004, J. Virol Methods, 122:9-15), with the following modifications. Extracts were prepared by homogenization of tissue in 50 mM Tris pH 7.4, 150 mM NaCl, 0.1% Triton X-100, and containing PMSV 1 MM and Chymostatin 10 μM as protease inhibitors. Soluble fractions were diluted to 0.2 mg/mL in PBS. Serial double dilutions of the tamples (100 μL) were made in round-bottomed 96-well microplate containing 100 μL of PBS. 100 μL of red blood chicken cells (2×10⁷ rbc/mL) (Innovative Research, South Field, Mich., USA) were added to each well. The plate was then incudated for 60-120 min at room temperature. Assay includes the following positive controls: rHA from PSC, ranged from 1 μg to 7.8 pg, diluted in PBS or spiked in non-transformed extract. A negative control using non-transformed extract was also run.

The hemagglutination assay was used to demonstrate the trimeric assembly of rHA fused to the coiled-coli peptides: That test, although very simple, is used on a routine basis to quantify the influenza titer. The principle of the assay is: free red blood cell roll will roll at the bottom an ELISA well, forming a cellular pile of red blood cells that can be easily detected. If hemagglutination occurs, the blood cell will form a matrix so the the blood cell can not roll at the bottom the ELISA well and no point can be seen. FIG. 11 shows that hemagglutination of chicken red blood cell can be performed directly on rHA expressed in a plant extract. More over the hemagglutination can occur with a plant extract expressing the rHA fused to GCN4-pII. Since the rHA monomer is unable to undergo red blood cell hemagglutination, that result ultimately demonstrates that the chimeric rHA assemble itself as a trimer in the plant.

Table 2 summarizes the sequences listed in the present application.

TABLE 2 Sequence description for sequence identifiers. SEQ ID NO: Sequence description 1 Amino acid sequence of the GCN4-pII peptide 2 peptide repeat of the PRD peptide of maize gamma-γ-Zein 3 tetrapeptide linker 4 SEKDEL ER retention signal 5 HDEL ER retention signal 6 amino acid sequence of the alfalfa PDI signal peptide 7 nucleotide sequence of the alfalfa PDI signal peptide 8 Amino acid sequence of mature HA 9 full length rHA, including the transmembrane domain, with the HA signal peptide replaced by the PDI signal peptide 10 SEQ ID NO: 9, with the transmembrane domain and cytoplasmic tail replaced by the retention signal SEKDEL 11 SEQ ID NO: 9, with the transmembrane domain and cytoplasmic tail replaced by the retention signal HDEL; 12 SEQ ID NO: 9, without the transmembrane domain and cytoplasmic tail 13 SEQ ID NO: 9, with the transmembrane domain and cytoplasmic tail replaced by the GCN4-pII peptide 14 SEQ ID NO: 13, with the SEKDEL retention signal at the C-terminus 15 SEQ ID NO: 9, with the transmembrane domain and cytoplasmic tail replaced by the PRD domain 16 SEQ ID NO: 15, with the SEKDEL retention signal at the C-terminus 17 the nucleotide sequence of the HA₀ gene fragment 18 the nucleotide sequence of the transmembrane domain and the cytoplasmic tail gene fragment 19 the nucleotide sequence of the ER-retained SEKDEL gene fragment. 20 the nucleotide sequence of the ER-retained HDEL gene fragment 21 the nucleotide sequence of the GCN4-pII gene fragment 22 the nucleotide sequence of the ER-retained GCN4-pII gene fragment 23 the nucleotide sequence of the PRD gene fragment 24 the nucleotide sequence of the ER-retained PRD gene fragment

The present invention has been described with regard to one or more embodiments. However, it will be apparent to persons skilled in the art that a number of variations and modifications can be made without departing from the scope of the invention as defined in the claims.

The contents of all references and patents cited throughout this application are hereby incorporated by reference in their entirety. 

1. A recombinant hemagglutinin (rHA), comprising: a) a hemagglutinin domain; and b) an oligomerization domain, wherein the rHA is produced as a chimeric soluble homotrimer.
 2. The rHA according to claim 1, wherein the protein further comprises a signal peptide.
 3. The rHA according to claim 1 or 2, wherein the protein further comprises an endoplasmic reticulum (ER) retention signal.
 4. A nucleotide sequence encoding the rHA of any one of claims 1 to
 3. 5. A nucleic acid sequence comprising: a) a nucleotide sequence encoding a hemagglutinin domain; and b) a nucleotide sequence encoding an oligomerization domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer.
 6. The nucleic acid sequence of claim 5, further comprising a nucleotide sequence encoding a signal peptide.
 7. The nucleic acid of claim 5 or 6, further comprising a nucleotide sequence encoding an endoplasmic reticulum (ER) retention signal.
 8. A vector comprising the nucleotide of any one of claims 4 to
 7. 9. A host cell expressing the rHA of any one of claims 1 to
 3. 10. A host cell transformed with the nucleotide of any one of claims 4 to
 7. 11. A host cell transformed with the vector of claim
 8. 12. A method of producing a recombinant rHA protein, comprising providing a host cell with a vector comprising: a) a nucleotide sequence encoding a hemagglutinin domain; and b) a nucleotide sequence encoding an oligomerization domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer.
 13. A method of expressing a recombinant hemagglutinin (rHA) within a plant comprising introducing a vector comprising: a) a nucleotide sequence encoding a hemagglutinin domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer; and b) a nucleotide sequence encoding an oligomerization domain, into a plant and expressing the rHA.
 14. The method of claim 13, wherein in the step of introducing (step a), the nucleic acid is introduced in the plant in a transient manner.
 15. The method of claim 13, wherein, in the step of introducing (step a), the nucleic acid is introduced in the plant so that it is stable.
 16. A method of producing a recombinant hemagglutinin (rHA) in a plant comprising: a) introducing a nucleic acid sequence into the plant, or portion thereof, the nucleic acid sequence comprising a regulatory region operatively linked to a nucleotide sequence encoding a hemagglutinin domain and an oligomerization domain, wherein the nucleic acid encodes a soluble rHA that forms a homotrimer; and b) growing the transgenic plant, thereby producing the rHA.
 17. The method of claim 16, wherein in the step of introducing (step a), the nucleic acid is introduced in the plant in a transient manner.
 18. The method of claim 16, wherein, in the step of introducing (step a), the nucleic acid is introduced in the plant so that it is stable. 